Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
July 26, 2026Orthopedic ReviewsOpen Access

The Association Between Charcot-Marie-Tooth Disease and Developmental Dysplasia of the Hip: A Narrative Review

View Full Paper
Ask AI
Bookmark
Share

Authors

KAKhalaf A. AlnowaishiriLALeen O. AlMutairiRARayan A. AlQarni

Discussion

Loading...

Member takes

Overview

Narrative review investigates the link between CMT and hip dysplasia in children, suggesting awareness is crucial.

Key Points

  • The review aims to explore the relationship between Charcot-Marie-Tooth disease and developmental dysplasia of the hip.
  • Systematic search of PubMed and Web of Science for articles on CMT and DDH in patients under 14 years.
  • Included 11 publications discussing patient characteristics, genetics, diagnosis, and treatment.
  • Evaluated incidence rates and diagnostic patterns among different CMT subtypes.
  • High incidence of hip dysplasia in CMT patients, with some studies reporting rates as high as 22%.
  • Genetic factors, including PMP22 gene duplication, influence the association between CMT and DDH.
  • Diagnosis involves physical exams, X-rays, and genetic tests to confirm both conditions.

Cite This Study

Alnowaishiri et al. (2026) studied this question.

synapsesocial.com/papers/6a65a825d3aea3239cd789fahttps://doi.org/10.52965/001c.163927
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Hip Dysplasia in Patients with Charcot-Marie-Tooth Disease: Unraveling an Underrecognized Condition2024
  2. 2Two Cases of Charcot-Marie-Tooth Disease Diagnosed in a 53-year-old Mother and a 24-year-old Daughter2025
  3. 3Genotypic and Phenotypic Characterization of Axonal Charcot–Marie–Tooth Disease in Childhood: Identification of One Novel and Four Known Mutations2025 · 1 citations
  4. 4Research Trends and Insights of Charcot–Marie–Tooth Disease (CMT): A Visualization Analysis (2000–2025)2026
  5. 5Novel Heterozygous Variant in a Child with Axonal Charcot–Marie–Tooth disease2026